Product NDC: | 51346-013 |
Proprietary Name: | BOTANICAL VANILLA PACT |
Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
Active Ingredient(s): | .55; 1.111; .319 g/11g; g/11g; g/11g & nbsp; TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51346-013 |
Labeler Name: | NATURE REPUBLIC CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120201 |
Package NDC: | 51346-013-01 |
Package Description: | 11 g in 1 CARTON (51346-013-01) |
NDC Code | 51346-013-01 |
Proprietary Name | BOTANICAL VANILLA PACT |
Package Description | 11 g in 1 CARTON (51346-013-01) |
Product NDC | 51346-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20120201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NATURE REPUBLIC CO., LTD. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .55; 1.111; .319 |
Strength Unit | g/11g; g/11g; g/11g |
Pharmaceutical Classes |